"atelosteogenesis" meaning in All languages combined

{
  "etymology_templates": [
    {
      "args": {
        "1": "en",
        "2": "atel-",
        "3": "osteogenesis"
      },
      "expansion": "atel- + osteogenesis",
      "name": "af"
    }
  ],
  "etymology_text": "From atel- + osteogenesis.",
  "forms": [
    {
      "form": "atelosteogeneses",
      "tags": [
        "plural"
      ]
    }
  ],
  "head_templates": [
    {
      "args": {
        "1": "~",
        "2": "atelosteogeneses"
      },
      "expansion": "atelosteogenesis (countable and uncountable, plural atelosteogeneses)",
      "name": "en-noun"
    }
  ],
  "lang": "English",
  "lang_code": "en",
  "pos": "noun",
  "senses": [
    {
      "categories": [
        {
          "kind": "other",
          "name": "English entries with incorrect language header",
          "parents": [
            "Entries with incorrect language header",
            "Entry maintenance"
          ],
          "source": "w"
        },
        {
          "kind": "other",
          "name": "English terms prefixed with atel-",
          "parents": [],
          "source": "w"
        },
        {
          "kind": "other",
          "name": "Pages with 1 entry",
          "parents": [],
          "source": "w"
        },
        {
          "kind": "other",
          "name": "Pages with entries",
          "parents": [],
          "source": "w"
        },
        {
          "kind": "topical",
          "langcode": "en",
          "name": "Pathology",
          "orig": "en:Pathology",
          "parents": [
            "Disease",
            "Medicine",
            "Health",
            "Biology",
            "Healthcare",
            "Body",
            "Sciences",
            "All topics",
            "Fundamental"
          ],
          "source": "w"
        }
      ],
      "examples": [
        {
          "ref": "2015 September 17, “Solute Carrier Family 26 Member a2 ( slc26a2 ) Regulates Otic Development and Hair Cell Survival in Zebrafish”, in PLOS ONE, →DOI:",
          "text": "Mutations in this gene are responsible for four recessively inherited chondrodysplasias, including diastrophic dysplasia, multiple epiphyseal dysplasia, atelosteogenesis type 2, and achondrogenesis 1B.",
          "type": "quote"
        }
      ],
      "glosses": [
        "incomplete osteogenesis; any pathological condition caused by this"
      ],
      "id": "en-atelosteogenesis-en-noun-cQEPNn0A",
      "links": [
        [
          "pathology",
          "pathology"
        ],
        [
          "incomplete",
          "incomplete"
        ],
        [
          "osteogenesis",
          "osteogenesis"
        ]
      ],
      "raw_glosses": [
        "(pathology) incomplete osteogenesis; any pathological condition caused by this"
      ],
      "tags": [
        "countable",
        "uncountable"
      ],
      "topics": [
        "medicine",
        "pathology",
        "sciences"
      ]
    }
  ],
  "word": "atelosteogenesis"
}

{
  "etymology_templates": [
    {
      "args": {
        "1": "en",
        "2": "atel-",
        "3": "osteogenesis"
      },
      "expansion": "atel- + osteogenesis",
      "name": "af"
    }
  ],
  "etymology_text": "From atel- + osteogenesis.",
  "forms": [
    {
      "form": "atelosteogeneses",
      "tags": [
        "plural"
      ]
    }
  ],
  "head_templates": [
    {
      "args": {
        "1": "~",
        "2": "atelosteogeneses"
      },
      "expansion": "atelosteogenesis (countable and uncountable, plural atelosteogeneses)",
      "name": "en-noun"
    }
  ],
  "lang": "English",
  "lang_code": "en",
  "pos": "noun",
  "senses": [
    {
      "categories": [
        "English countable nouns",
        "English entries with incorrect language header",
        "English lemmas",
        "English nouns",
        "English nouns with irregular plurals",
        "English terms prefixed with atel-",
        "English terms with quotations",
        "English uncountable nouns",
        "Pages with 1 entry",
        "Pages with entries",
        "en:Pathology"
      ],
      "examples": [
        {
          "ref": "2015 September 17, “Solute Carrier Family 26 Member a2 ( slc26a2 ) Regulates Otic Development and Hair Cell Survival in Zebrafish”, in PLOS ONE, →DOI:",
          "text": "Mutations in this gene are responsible for four recessively inherited chondrodysplasias, including diastrophic dysplasia, multiple epiphyseal dysplasia, atelosteogenesis type 2, and achondrogenesis 1B.",
          "type": "quote"
        }
      ],
      "glosses": [
        "incomplete osteogenesis; any pathological condition caused by this"
      ],
      "links": [
        [
          "pathology",
          "pathology"
        ],
        [
          "incomplete",
          "incomplete"
        ],
        [
          "osteogenesis",
          "osteogenesis"
        ]
      ],
      "raw_glosses": [
        "(pathology) incomplete osteogenesis; any pathological condition caused by this"
      ],
      "tags": [
        "countable",
        "uncountable"
      ],
      "topics": [
        "medicine",
        "pathology",
        "sciences"
      ]
    }
  ],
  "word": "atelosteogenesis"
}